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6,7-bis(3,4-bis(dodecyloxy)phenyl)-2-dodecyl-4,9-bis(4-(2-ethylhexyl) thiophen-2-yl)-2H-[1-3]triazolo[4,5-g]quinoxaline | 1450617-44-3

中文名称
——
中文别名
——
英文名称
6,7-bis(3,4-bis(dodecyloxy)phenyl)-2-dodecyl-4,9-bis(4-(2-ethylhexyl) thiophen-2-yl)-2H-[1-3]triazolo[4,5-g]quinoxaline
英文别名
6,7-Bis(3,4-didodecoxyphenyl)-2-dodecyl-4,9-bis[4-(2-ethylhexyl)thiophen-2-yl]triazolo[4,5-g]quinoxaline;6,7-bis(3,4-didodecoxyphenyl)-2-dodecyl-4,9-bis[4-(2-ethylhexyl)thiophen-2-yl]triazolo[4,5-g]quinoxaline
6,7-bis(3,4-bis(dodecyloxy)phenyl)-2-dodecyl-4,9-bis(4-(2-ethylhexyl) thiophen-2-yl)-2H-[1-3]triazolo[4,5-g]quinoxaline化学式
CAS
1450617-44-3
化学式
C104H169N5O4S2
mdl
——
分子量
1617.65
InChiKey
GEAJSUROUIOFAF-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    42.2
  • 重原子数:
    115
  • 可旋转键数:
    75
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    150
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    6,7-bis(3,4-bis(dodecyloxy)phenyl)-2-dodecyl-4,9-bis(4-(2-ethylhexyl) thiophen-2-yl)-2H-[1-3]triazolo[4,5-g]quinoxalineN-溴代丁二酰亚胺(NBS) 作用下, 以 氯仿 为溶剂, 以47%的产率得到6,7-bis(3,4-bis(dodecyloxy)phenyl)-4,9-bis(5-bromo-4-(2-ethylhexyl)thiophen-2-yl)-2-dodecyl-2H-[1-3]triazolo[4,5-g]quinoxaline
    参考文献:
    名称:
    Synthesis and photovoltaic performance of novel thiophenyl-methylene-9H-fluorene-based low bandgap polymers
    摘要:
    Three novel donor-acceptor polymers have been synthesized with Suzuki cross-coupling between thiophenyl-methylene-9H-fluorene donating unit with thiazolo[5,4-d]]thiazole (PHI benzothiadiazole (PFTODTBT) or [1,2,3]triazolo[4,5-g]quinoxaline (PFTDTBTzQ) accepting unit. The polymer PFTTTz-THF prepared from tetrahydrofuran (THF) presented higher molecular weight and narrower polydiversity than that from toluene (PFTTTz-toluene), leading to higher photovoltaic performance in BHJ devices of these polymers blended with PC71BM ([6,6]-phenyl-C-71-butyric acid methyl ester). These good solution processable polymers exhibit a bandgap of 1.66-1.93 eV and a low highest occupied molecular orbital (HOMO) energy level similar to -5.32 eV. Polymers PFTTTz and PFTODTBT displayed strong absorption in the range of 300-650 nm, while PFTDTBTzQ showed a further 100 nm extended absorption band. Overall efficiencies over 1.5% are achieved for BHJ devices fabricated from blends of PFTITz with PC71BM as active layer. A maximum power conversion efficiency of 2.21% is obtained by the use of interlayer poly [(9,9-dioctyl-2,7-fluorene)-alt-(9,9-bis(3'-(N, N-dimethylamino)propyl)-2,7-fluorene)] (PFN) and Ca between active layer and Al anode. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.polymer.2013.07.001
  • 作为产物:
    描述:
    2-dodecyl-4,7-bis(4-(2-ethylhexyl)thiophen-2-yl)-2H-benzo[d] [1-3]triazole- 5,6-diamine1,2-bis(3,4-bis(dodecyloxy)phenyl)ethane-1,2-dione溶剂黄146 作用下, 反应 24.0h, 以95%的产率得到6,7-bis(3,4-bis(dodecyloxy)phenyl)-2-dodecyl-4,9-bis(4-(2-ethylhexyl) thiophen-2-yl)-2H-[1-3]triazolo[4,5-g]quinoxaline
    参考文献:
    名称:
    Synthesis and photovoltaic performance of novel thiophenyl-methylene-9H-fluorene-based low bandgap polymers
    摘要:
    Three novel donor-acceptor polymers have been synthesized with Suzuki cross-coupling between thiophenyl-methylene-9H-fluorene donating unit with thiazolo[5,4-d]]thiazole (PHI benzothiadiazole (PFTODTBT) or [1,2,3]triazolo[4,5-g]quinoxaline (PFTDTBTzQ) accepting unit. The polymer PFTTTz-THF prepared from tetrahydrofuran (THF) presented higher molecular weight and narrower polydiversity than that from toluene (PFTTTz-toluene), leading to higher photovoltaic performance in BHJ devices of these polymers blended with PC71BM ([6,6]-phenyl-C-71-butyric acid methyl ester). These good solution processable polymers exhibit a bandgap of 1.66-1.93 eV and a low highest occupied molecular orbital (HOMO) energy level similar to -5.32 eV. Polymers PFTTTz and PFTODTBT displayed strong absorption in the range of 300-650 nm, while PFTDTBTzQ showed a further 100 nm extended absorption band. Overall efficiencies over 1.5% are achieved for BHJ devices fabricated from blends of PFTITz with PC71BM as active layer. A maximum power conversion efficiency of 2.21% is obtained by the use of interlayer poly [(9,9-dioctyl-2,7-fluorene)-alt-(9,9-bis(3'-(N, N-dimethylamino)propyl)-2,7-fluorene)] (PFN) and Ca between active layer and Al anode. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.polymer.2013.07.001
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